Diphenyl diselenide - ≥96% , CAS No.1666-13-3

CAS: 1666-13-3 Cat. No.: D106407 Peso molecular: 312.13 Beilstein Registry Number: 2047179 Número EC: 216-780-2

GRADE & PURITY ≥96%

Synonyms

1,2-Diphenyldiselane | Q3538196 | Diphenyl diselenide, 98% | 9ATU3Z459Q | DTXSID6061864 | 1,2-Diphenyldiselane # | A810750 | AC-11061 | InChI=1/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10 | C12H10Se2 | NSC49763 | NSC-49763 | UNII-9ATU3Z459Q | D

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Descripción general

Diphenyl diselenide (Ph2Se2) is an organoselenium compound. Its crystalline structure, toxicokinetic properties,antioxidant and anti-inflammatory activities have been investigated. Its ability to reverse the oxidative brain damage and mitochondrial dysfunction induced by acetaminophen has been studied in mice. It reacts with thallium (Tl) to form TI (SePh). It participates in a four-component radical coupling to form substituted cyclopentanes.
Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro.

Specifications

Sinónimos

1, 2-Diphenyldiselane | Q3538196 | Diphenyl diselenide, 98% | 9ATU3Z459Q | DTXSID6061864 | 1, 2-Diphenyldiselane # | A810750 | AC-11061 | InChI=1/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10 | C12H10Se2 | NSC49763 | NSC-49763 | UNII-9ATU3Z459Q | D

Especificaciones y pureza

≥96%

Mecanismos bioquímicos y fisiológicos

Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro.

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

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Tipo de acción

INHIBITOR

Pureza

≥96%

Nombres e identificadores

• Sonrisas canónicas: C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
• IUPAC Name: (phenyldiselanyl)benzene
• InChIKey: YWWZCHLUQSHMCL-UHFFFAOYSA-N
• INCHI: 1S/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
• Isómeros SMILES: C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
• WGK Alemania: 3
• RTECS: JM9152500
• Número ONU: 3283
• Peso molecular: 312.13
• Beilstein: 2047179
• Reaxy-Rn: 2047179
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2047179&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organoselenium compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Hydrocarbon derivative - Organoselenium compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 (1 Activities)

Discover Target: EHMT2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

EHMT1 Tchem Histone-lysine N-methyltransferase EHMT1 (1 Activities)

Discover Target: EHMT1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HT-29 (80576 Activities)

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SH-SY5Y (11521 Activities)

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EHMT1 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 5 (407 Activities)

Discover Target: EHMT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Aspergillus (103 Activities)

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Candida albicans (78123 Activities)

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Fusarium (166 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Insoluble in water, soluble in toluene
• Sensibilidad: Moisture &air sensitive
• Punto de ebullición (°C): 202°C/11mmHg
• Punto de fusión (°C): 60-63°C
• Peso molecular: 312.100 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 313.911 Da
• Monoisotopic Mass: 313.911 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 128.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

XLogP3

Referencias

1. Linzhi Shen, Ziwen Xiong, Zhaohui Du, Hao Wang, Wenrui Li, Zhen Zhang, Hao Wu, Changsong Zhou, Yaming Zhou, Guanghua Tang, Jing Liu, Hongmin Yang.  (2023)  Unveiling the electron-acceptor effect in selenium-doped Cu-N-C catalyst with atomically dispersed active sites for boosting Hg0 oxidation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.126078]

2. Chengfei Liu, Banruo Xianyu, Yiheng Dai, Shuojiong Pan, Tianyu Li, Huaping Xu.  (2023)  Intracellular Hyperbranched Polymerization for Circumventing Cancer Drug Resistance.  ACS Nano,      [PMID:37285408] [10.1021/acsnano.3c03512]

3. Jianfa Chen, Chong Lin, Mengmeng Zhang, Tianxiang Jin, Yong Qian.  (2020)  Constructing Nitrogen, Selenium Co-Doped Graphene Aerogel Electrode Materials for Synergistically Enhanced Capacitive Performance.  ChemElectroChem,  7  (15): (3311-3318).  [PMID:] [10.1002/celc.202000635]

4. Jia Liu, Xiaoning Ma, Yanping Tong, Meidong Lang.  (2018)  Syntheses of diselenide-containing dynamic polymers and their application in polymer alloys.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2018.10.154]

5. Shenjie Li, Daocheng Pan.  (2012)  Cu2SnSe3 and alloyed (ZnSe)x(Cu2SnSe3)1−x nanocrystals with a metastable zincblende and wurtzite structure.  JOURNAL OF CRYSTAL GROWTH,      [PMID:] [10.1016/j.jcrysgro.2012.07.045]

6. Kewei Gu, Tingting Wang, Guowei Yang, Nan Yu, Chengchao Du, Junli Wang.  (2024)  Inorganic–Organic Hybrid Layered Semiconductor AgSePh: Quasi-Solution Synthesis, Optical Properties, and Thermolysis Behavior.  INORGANIC CHEMISTRY,      [PMID:38528435] [10.1021/acs.inorgchem.4c00343]

7. Jinlin Wang, Can Wu, Wang Zhang, Yang Zhao, Kai Ding, Jie Xiao, Xiaoyuan Zeng, Yingjie Zhang.  (2025)  Promoting polysulfide conversion by catalytic of ZnSe nanoparticles for room-temperature sodium-sulfur battery.  Journal of Energy Storage,      [PMID:] [10.1016/j.est.2025.116374]

8. Yu Qiao, Wenzhong Ma, You Zhang, Tiansheng Gao, Haicun Yang, Zheng Cao, Jing Zhong.  (2024)  Ultra-high stretchability and shape fixation rate shape memory polyurethanes based on cyclic polytetrahydrofuran molecular rings.  POLYMER,      [PMID:] [10.1016/j.polymer.2024.127578]